Di-Zhao Chen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Di-Zhao Chen has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
Hai-Feng Wu
B Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education , Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College , Beijing , PR China
2 shared publicationsGuo-Xu Ma
B Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education , Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College , Beijing , PR China
1 shared publicationJing Zhou
A Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, Department of Chemistry & Chemical Engineering , Huaihua University , Huaihua , PR China
1 shared publicationQiong-Yu Zou
A Key Laboratory of Hunan Province for Study and Utilization of Ethnic Medicinal Plant Resources, Department of Chemistry & Chemical Engineering , Huaihua University , Yingfeng East Road, Huaihua , Hecheng District, Hunan 418008 , P.R. China
1 shared publication- Qiongyu Zou
Key Laboratory of Research and Utilization of Ethnomedicinal Plant Resources of Hunan Province, Key Laboratory of Hunan Higher Education for Western Hunan Medicinal Plant and Ethnobotany, Hunan Provincial Higher Education Key Laboratory of Intensive Processing Research On Mountain Ecological Food, Key Laboratory of Natural Products Research and Utilization in Wuling Mountain Area, Department of Chemistry & Chemical Engineering, Huaihua University, China
1 shared publication Xin Liu
C Beijing Entry-Exit Inspection and Quarantine Bureau , Beijing , PR China
1 shared publication
Latest Publications
- 13 April 2017
- Published by Taylor & Francis in Natural Product Research
- Vol. 31 (21) , 2484-2490
A new cycloartane triterpenoid glycoside from Souliea vaginata
One new cycloartane triterpenoid glycoside, soulieoside Q (1), together with four known compounds (2−5) were isolated from the ethanolic extract of the rhizomes of Souliea vaginata Maxim. The structure of the new compound was determined by extensive spectroscopic analysis including 1D and 2D NMR and HRESIMS, as well as chemical methods. Compound 1 was evaluated for its cytotoxic activities against HepG2 and A549 cancer cell lines. Graphical Abstract
- 13 April 2017
- Published by Taylor & Francis in Natural Product Research
- Vol. 31 (21) , 2484-2490
A new cycloartane triterpenoid glycoside from Souliea vaginata
One new cycloartane triterpenoid glycoside, soulieoside Q (1), together with four known compounds (2−5) were isolated from the ethanolic extract of the rhizomes of Souliea vaginata Maxim. The structure of the new compound was determined by extensive spectroscopic analysis including 1D and 2D NMR and HRESIMS, as well as chemical methods. Compound 1 was evaluated for its cytotoxic activities against HepG2 and A549 cancer cell lines. Graphical Abstract
- 20 July 2015
- Published by Taylor & Francis in Natural Product Research
- Vol. 30 (1) , 1-6
A new labdane diterpene from the rhizomes of Alpinia officinarum
A new labdane diterpene, (Z)-12,14-labdadien-15(16)-olide-17-oic acid (1), and a new natural cadinane sesquiterpene, 4-isopropyl-6-methyl-1-naphthalenemethanol (2), were isolated from the ethanolic extract of the rhizomes of Alpinia officinarum, together with three other products, galangin (3), kaempferol (4) and quercetin (5). Their structures were elucidated by using extensive spectroscopic methods. Compounds 1 and 2 showed no remarkable cytotoxic activity against HeLa and HepG2 cancer cell lines with IC50>50 μg mL− 1.
- 20 July 2015
- Published by Taylor & Francis in Natural Product Research
- Vol. 30 (1) , 1-6
A new labdane diterpene from the rhizomes of Alpinia officinarum
A new labdane diterpene, (Z)-12,14-labdadien-15(16)-olide-17-oic acid (1), and a new natural cadinane sesquiterpene, 4-isopropyl-6-methyl-1-naphthalenemethanol (2), were isolated from the ethanolic extract of the rhizomes of Alpinia officinarum, together with three other products, galangin (3), kaempferol (4) and quercetin (5). Their structures were elucidated by using extensive spectroscopic methods. Compounds 1 and 2 showed no remarkable cytotoxic activity against HeLa and HepG2 cancer cell lines with IC50>50 μg mL− 1.